NDC 68001-483 Triple Antibiotic

First Aid Antibiotic

NDC Product Code 68001-483

NDC 68001-483-45

Package Description: 1 TUBE in 1 CARTON > 28000 mg in 1 TUBE

NDC 68001-483-46

Package Description: 1 TUBE in 1 CARTON > 14000 mg in 1 TUBE

NDC Product Information

Triple Antibiotic with NDC 68001-483 is a a human over the counter drug product labeled by Bluepoint Laboratories. The generic name of Triple Antibiotic is first aid antibiotic. The product's dosage form is ointment and is administered via topical form.

Dosage Form: Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Triple Antibiotic Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.


Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WHITE PETROLATUM (UNII: B6E5W8RQJ4)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Bluepoint Laboratories
Labeler Code: 68001
FDA Application Number: part333B What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 06-15-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Triple Antibiotic Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Other

Drug Facts

Active Ingredients

Bacitracin Zinc (400 units in each gram)Neomycin Sulfate 5mg (equivalent to 3.5mg Neomycin per gram)Polymyxin B Sulfate (5000 units per gram)

Purpose

First Aid Antibiotics

Uses

First Aid to help prevent infection in minor cuts, scrapes and burns

Warnings

For external use only.

Do Not Use

  • Do not useIn the eyes or apply over large areas of the bodyIf you are allergic to any of the ingredientsLonger than 1 week unless directed by a doctor

Otc - When Using

Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns

Otc - Stop Use

Stop use and ask a doctor if the condition persists or gets worse, or if a rash or other allergic reaction develops

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Clean the affected area. Apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily. May be covered with a sterile bandage.

Other Information

  • Preserve in well-closed containersStore at room temperatue

Inactive Ingredients

White Petrolatum

Questions?

Contact 1-800-707-4621Manufactured in India by:Gopaldas Visram & Company Limited.Plot No. A327, T.T.C. Indl. Area, M.L.D.C.Mahape, Navi Mumbai - 400710.Mfg. Lic. No.: KD/503For BluePoint LaboratoriesRev 05/2021

* Please review the disclaimer below.